A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561463



Internal ID334443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131507269..131904335hg38UCSC Ensembl
chr6:131828409..132225475hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38397067
hg19397067
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969141
Samples
Known GenesARG1, CTAGE9, ENPP1, ENPP3, MED23, OR2A4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561463
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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